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Study of the Size of the Operating Fields Depending on the Morphology of the Patients (ABORD-3D)

G

Geprovas

Status

Completed

Conditions

Open Surgery on the Abdominal Aorta

Treatments

Procedure: open surgery on the abdominal aorta by laparotomy

Study type

Observational

Funder types

NETWORK

Identifiers

NCT06063395
2023-A01613-42

Details and patient eligibility

About

This is a prospective, single-centre, observational clinical study.

Patients who have not expressed their non-opposition, who are of age and who are undergoing open surgery on the abdominal aorta by laparotomy will be included.

The aim is to mathematically model the working volume for abdominal aortic surgery as a function of the preoperative CT scan, the length and orientation of the incision and the morphometric characteristics of the patient, and thus predict the surgical risk.

To meet this objective, the dimensions of the working volume of open abdominal aortic surgery will be measured using a camera to create an algorithm by associating them with the preoperative images and morphometric data of the patient.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients over 18 years of age
  • Patient undergoing open surgery on the abdominal aorta by laparotomy.
  • Patient who has been informed of the terms of the study and who has not expressed non-opposition.

Exclusion criteria

  • Emergency surgery
  • Patient without preoperative CT scan

Trial design

30 participants in 1 patient group

Patient undergoing open surgery on the abdominal aorta by laparotomy
Treatment:
Procedure: open surgery on the abdominal aorta by laparotomy

Trial contacts and locations

1

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Central trial contact

Manon Ruhlmann; Maxime BEUTELSTETTER

Data sourced from clinicaltrials.gov

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